Cooling agent

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

[0001] The present invention relates to a cooling agent and more particularly pertains to a cooling agent having an excellent cooling property and an agreeable touch, free from conglomerating in the state of crystal, and realizing such a cooling product that has no fear of unagreeable feel or breakage of the covering bag when used for cooling down the head or affected parts, but has a high comfortability and safety, and also to a cooling pillow utilizing the cooling agent.

2. Description of the Related Art

[0002] Heretofore, in order to cool down the head and affected parts, ice-bags or water pillows have conventionally been used.

[0003] Lately, cooling pillows utilizing endothermic phenomena caused from dissolution of crystals of inorganic salts into water as solvent have been distributed, and as the content thereof, cooling agent comprising sodium sulfate and water or disodium hydrogenphosphate and water in combination are known (Japanese Utility Model Publication No. 21809/1992).

[0004] Ice-bags and water pillows are, however, generally large in weight, and meet many inconveniences including the necessity of preparing ice or cold water for every use.

[0005] A cooling bag comprising an inorganic salt, specifically an inorganic ammonium salt and/or an alkaline metallic salt, and a salt hydrate containing at least a hydrate of strontium hydroxide is known from the document EP 0 498 428 A1.

[0006] Cooling agents comprising sodium sulfate and water or disodium hydrogenphosphate and water in combination are superior in convenience to ice bags and water pillows, but have many defects. Once they are dissolved and then recrystallize, the crystals become larger in particle size to offer poor touch at serving and cause discomfort. Further, the crystals conglomerate when left as it is, and the resulting stiff crystals sometimes break the bag containing the cooling agent by shock.

SUMMARY OF THE INVENTION

[0007] To overcome these problems, the present inventors repeated investigations to obtain a cooling agent provided with safety, agreeable touch and cooling feel free from conglomerating at crystallization and consequently found that these problems can be overcome by using sodium phosphate salt and sodium ammonium phosphate salt or ammonium phosphate salt, in combination, as the inorganic salts crystallizing at around room temperature. Thus, the present invention has been attained.

[0008] That is, the present invention relates to the use of (i) at least a sodium phosphate salt selected from disodium hydrogenphosphate, sodium dihydrogenphosphate, trisodium phosphate and hydrates thereof, (ii) at least one sodium ammonium phosphate salt or one ammonium phosphate salt selected from sodium ammonium hydrogenphosphate, diammonium hydrogenphosphate, ammonium dihydrogenphosphate, ammonium phosphate and hydrates thereof, and (iii) water in a cooling agent composition containing 5 to 60% by weight of the phosphate salts as the anhydride form, and also a cooling pillow using the same.

DESCRIPTION OF PREFERRED EMBODIMENT

[0009] In the cooling agent of the present invention, sodium-containing phosphate salts and ammonium-containing phosphate salts are used in combination, as the inorganic salts for the cooling agent mixed with water, and usually sealed in a flat bag to be put into practical use.

[0010] Examples of sodium phosphate salts to be used in the present invention are disodium hydrogenphosphate (Na₂HPO₄), 12H₂O hydrate thereof, sodium dihydrogenphosphate (NaH₂PO₄), 2H₂O hydrate thereof, trisodium phosphate (Na₃PO₄), and 10H₂0 hydrate thereof. Among them, preferred are disodium hydrogenphosphate and hydrates thereof as the main component.

[0011] Sodium ammoniumphosphate salts or ammonium phosphate salts to be used in combination with the above-mentioned sodium phosphate salts are, for example, sodium ammonium hydrogenphosphate (NaNH₄HP0₄), 4H₂O hydrate thereof, diammonium hydrogenphosphate [(NH₄)₂HP0₄], ammonium dihydrogenphosphate (NH₄H₂PO₄), triammonium phosphate [(NH₄)₃PO₄], and hydrates thereof. Among them, preferred are sodium ammonium hydrogenphosphate, diammonium hydrogenphosphate, and hydrates thereof as the main component.

[0012] Generally, cooling agents are prepared by mixing a sodium phosphate salt and a sodium ammonium hydrogenphosphate salt or an ammonium phosphate salt itself as mentioned above with water, or by heat dissolving and then recrystallizing them, but mostly the former method are adopted. Or an acid, an alkali and a salt which react in water to produce them may be mixed and used as a cooling agent.

[0013] For example, to produce sodium phosphate salts containing disodium hydrogenphosphate as the main component, used are (i) a method of neutralizing phosphoric acid with caustic soda or sodium carbonate, or (ii) a method of adding phosphoric acid to the aqueous solution of anhydrous sodium phosphate salts such as trisodium triphosphate (Na₃P₃O₉), trisodium phosphate (Na₃PO₄), sodium dihydrogenphosphate (NaH₂PO₄), sodium pyrophosphate (NaP₂O₇), disodium dihydrogenpyrophosphate (Na₂H₂P₂O₇), sodium methaphosphate [(NaPO₃)_n], sodium tripolyphosphate (Na₅P₃O₁₀) and hydrate-containing salts thereof.

[0014] To prepare ammonium salts containing sodium ammonium hydrogenphosphate salts as the main component, for example, (i) a method of adding ammonium chloride to the aqueous solution of disodium hydrogenphosphate, (ii) a method of adding caustic soda to the aqueous solution of anhydrous phosphate salt such as ammonium dihydrogenphosphate, diammonium hydrogenphosphate, triammonium phosphate and hydrate-containing salts thereof, and (iii) a method of preparing ammonium phosphate salts from phosphoric acid and aqueous ammonia, and further taking the above-mentioned step (ii) are adopted.

[0015] In these methods, depending on the conditions for preparation, also other sodium phosphate salts or ammonium phosphate sometimes are produced in a mixed state, but they can be used as it is as the cooling agent.

[0016] In the cooling agent of the present invention, the concentration and compounding proportions of the salts are selected so that crystals will be precipitated in a lower range of room temperature, that is, at a temperature of 10 to 25 °C, and the precipitated crystal can be dissolved with endothermic phenomena in a temperature range where the temperature of it is raised by the person's temperature and the like, that is, for example, a temperature of 25 to 30 °C.

[0017] The amount by weight of the salts in total of sodium phosphate salts and sodium ammonium phosphate salts or ammonium phosphate salts is, if the amount in total of the salts in aqueous solution and in the form of the precipitating crystal, as anhydride thereof, usually 5 to 60% by weight, preferably 15 to 35% by weight, and still more preferably 20 to 30% by weight of whole the amount of. the cooling agent.

[0018] If the amount by weight of salts is lower than 5% by weight, it is difficult for them to recrystallize at room temperature, while if it is larger than 60% by weight, the amount of crystal is so large that the touch of the cooling agent may be unfavorably lowered.

[0019] The proportion of the sodium ammonium hydrogenphosphate and the ammonium phosphate salts to the sodium phosphate salt is not particularly limited, but the ratio of Na to NH₄ group (Na/NH₄) contained in whole the phosphate in the cooling agent is usually 1 : 5 to 5 : 1, preferably 1 : 1 to 5 : 1 in molar ratio, and the total molar ratio of Na and NH₄ group to 1 mol of PO₄ group, that is, [(Na+NH₄)/PO₄)] is usually 1 : 1.5 to 1 : 2.5, preferably 1 : 1.8 to 1 : 2.2. If the ratio of Na and NH₄ group and PO₄ group is too distant from these ranges, there is the possibility that the crystalline particles become too large, or conglomerate, or pH of the solution becomes 10 or more or 4 or less, which causes problems in safety in handling at production.

[0020] In the present invention, for the purpose of controlling the amount of precipitating crystal and the dissolution temperature of the cooling agent, in addition to the above-mentioned salts, other salts can be used in combination, if necessary. For example, sodium carbonate, sodium hydrogencarbonate, potassium sodium carbonate, sodium chrome carbonate, sodium scandium carbonate, sodium cerium carbonate, and sodium sulfate, and hydrates thereof can be used.

[0021] In the present invention, it is preferred to add nucleating agents to help the precipitation of crystal.

[0022] As nucleating agent, phosphates or hydroxides of the metals such as lithium and alkaline earth metals, and hydrates of these compounds are used.

[0023] The phosphates include strontium phosphates, lithium phosphates, calcium phosphates, barium phosphates, and magnesium phosphates, and hydrates thereof. Specific examples of them are trilithium phosphate, dilithium hydrogenphosphate, lithium di hydrogen phosphate, tristrontium diphosphate, strontium hydrogenphosphate, strontium tetrahydrogendiphosphate, tri calcium diphosphate, calcium hydrogenphosphate, calcium tetrahydrogendiphosphate, trimagnesium diphosphate, magnesium hydrogen phosphate, magnesium tetrahydrogendi phosphate, tribarium diphosphate, barium hydrogenphosphate, barium tetrahydrogendiphosphate, and hydrates thereof. Besides the above, pyrophosphates which are hydrolyzed in water to produce these salts are also effective.

[0024] The hydroxide includes strontium hydroxide, calcium hydroxide, lithium hydroxide, barium hydroxide, and magnesium hydroxide, and hydrates thereof.

[0025] Among them, calcium phosphates, strontium phosphates, calcium hydroxide, and strontium hydroxide, and hydrates thereof are preferable, and calcium hydrogenphosphate, strontium hydrogenphosphate, strontium hydroxide, and hydrates thereof are particularly preferable. These may be used alone, or two or more of them may be used in combination.

[0026] By adding and mixing these nucleating agents, usually fine and stable precipitation of crystal is obtained. When a hydroxide is used, however, it is preferably heated to about 80°C once after added, then cooled, and thus made into a still finer crystalline precipitation before used.

[0027] The amount of the nucleating agent is 0.01 to 5% by weight, preferably 0.05 to 3% by weight in respect of the whole cooling agent.

[0028] In the present invention, it is preferred to add highly water absorbent polymer, thickener, polymeric flocculant for the purpose of preventing the cooling agent from conglomerating, constantly maintaining it in a state of fine crystal to offer a soft touch, and at the same time heightening the safety so that the chemical solution may not scatter onto human body even if the bag is broken.

[0029] The highly water absorbent polymer include, for example, polyacrylic acid, starch-acrylic acid graft copolymer, maleic acid copolymer, polyvinyl alcohol, and isobutylene-maleic acid copolymer. The thickener includes, for example, xanthan gum (polysaccharide), carboxymethylcellulose and sepiolite clay. As the polymeric flocculant, any of cationic, anionic, nonionic, ampho-ionic (including betainic ampho-ionic) ones can be used. Specific examples of them are polymethacrylic acid ester, polyallyl amine, polyacrylamide, chitosan, polyacrylic soda, acrylamide-acrylic soda copolymer, partially hydrolyzed polyacrylamide, and polyethyleneoxide. These may be used alone, or two or more of them may be used in combination.

[0030] Among them, highly water absorbent polymer and polysaccharide-based thickeners are preferable, and preferable example of the former are polyacrylic highly water absorbent polymer such as SANWET^R IM-500D, and SANFRESH^R ST-500MPS (produced by SANYO CHEMICAL INDUSTRIES,LTD.), AQUALIC^R CS 6S, and AQUALIC^R CS 6HM (produced by NIPPON SHOKUBAJ CO.,LTD.), particularly those in fine particle such as SANFRESH^R ST-500MPS and AQUALIC^R CS 6S, and preferable example of the latter are KELZAN^R (xanthan gum produced by KELCO DIVISION OF MERCK & CO.,INC. U.S.)

[0031] The amount of them to be added is usually 0.01 to 3% by weight, preferably 0.1 to 2% by weight in respect of the whole cooling agent.

[0032] The present invention further includes an invention relating to a cooling pillow using the above-mentioned cooling agent.

[0033] A cooling pillow herein means a cooling pillow, in general sense, which comprises the above-mentioned cooling agent sealed in a water-penetration resistant bag, and which is to be applied on a hot part to cool said part, and is effectively utilized as the cooling bag to cool down affected parts, and as temperature-controlling means fixed on the warm part of industrial equipments, as well as the usual use as a cooling pillow for men.

[0034] As the material for the bag which contains the cooling agent, synthetic resin films of polyethylene, polypropylene, polyester, nylon, polyvinyl chloride, polyvinylidene chloride, and polyisocyanate, and combinated films thereof can be used . Among them, films of polyvinyl chloride, nylon and combination thereof are preferable in view of strength, flexibility, processability and cost.

[0035] Cooling pillows are usually made by putting the cooling agent into a flat bag, but in the case of cooling pillow for men, for-the purpose of providing superior touch, realizing comfortable sleep, and enhancing the recovery from fatigue, both or one side of the outer surface of the synthetic resin film bag may be covered with, or laminated by absorbent cotton, gauze, nonwoven fabric made of water-absorbing fiber layer, or fiber-planted cloth with water-absorbing fiber layer planted on it.

[0036] The flat bag which contains the cooling agent is used as a cooling pillow, as it is, or further covered with soft covering material, or contained in a thick pillow provided with containing part such as a pocket. The size and shape of the flat bag are not particularly limited, but are sufficient as large as the bag has an area size enough to be applied to the above-mentioned purposes. The shape of it may be any of rectangle, square, circle or oval.

[0037] Cooling pillows or cooling bags thus obtained are used in the state in which a large amount of fine crystals are precipitated out at a temperature of 10 to 25 °C. The cooling agent absorbs heat of the head of the patient while cooling it, and the rise in the temperature of it owing to the absorption dissolves the crystal again. During the dissolution, since absorption of heat caused by dissolution is kept, desired temperature of 25 to 30 °C is maintained to offer favorable feel for a long period of time. After they are used, the pillow or bag can be further used repeatedly, for the cooling agent crystallizes again when they are left under a low temperature atmosphere of 10 to 25 °C.

[0038] The cooling agent of the present invention is obtained from the co-use of a sodium phosphate salt and an ammonium phosphate salt, and is free from conglomerating of crystal which has been the defect of prior arts. Thus, it can be repeatedly used for many times.

[0039] If a nucleating agent, a highly water absorbent polymer, or a thickener is added to the cooling agent, a still stabler state of finer crystal precipitation is maintained.

[0040] Accordingly, said cooling agent, in an application to cooling pillows has an excellent cooling agent property and offers soft and favorable touch, comfortability with safety, without the fear of conglomerating of crystals even after left for a long period of time, and can be used repeatedly with safety.

EXAMPLE 1

[0041] Two sheets of colorless semitransparent soft polyvinyl chloride film with a thickness of 90µm cut to the size of 220 x 240 mm were overlapped, three sides of which were high-frequency stitched each in the width of 5 mm to make a flat bag with one side open.

[0042] Into said bag, placed a cooling agent which was obtained by adding ion-exchanged water to 162 g, as anhydride, of disodium hydrogenphosphate, and 162 g, as anhydride, of sodium ammonium hydrogenphosphate to make a mixture of 1300 g in total, and the open side was sealed by high-frequency stitching to obtain a cooling pillow.

[0043] Said cooling pillow was immersed in a thermostat water bath of 30 °C, and the crystals therein were dissolved.

[0044] Thereafter, the cooling pillow was left in a room at 10 °C overnight, and crystals were precipitated again. Said crystals were fine and in a slurry state, and the whole pillow was soft and-had a favorable touch.

[0045] Subsequently, one side surface of the above cooling pillow was made to closely contact with the outer wall of the thermostat water bath kept at 30 °C, a thermocouple thermometer was set onto the other side surface, which was covered all over with three-fold flannel, firmly fixed with sticky tape, and the change in the temperature was measured.

[0046] As the result, the temperature of the pillow rose while the crystals dissolved little by little. The favorable temperature for a comfortable pillow was maintained for a long period of time as about 8 hours corresponding to the change in the temperature from 10 °C to 25 °C, and 114 hours in total till the temperature reached 28 °C.

[0047] The sample was left in a room at 10 °C again to precipitate crystals, and the state was observed. As the result, the crystals were found to be fine, and the cooling agent was in a slurry state. The sample was left as it is for one week, but the state hardly changed, and no conglomeration was observed.

[0048] As the result of further observation, crystals with a particle diameter of 3 to 6 mm were found in some parts only after 5 days.

EXAMPLE 2

[0049] A sample of a cooling pillow was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 240 g, as anhydride, of disodium hydrogenphosphate and 78 g, as anhydride, of diammonium hydrogenphosphate to make a mixture of 1300 g in total.

[0050] As the result of carrying out a test on the sample under the same conditions as in Example 1, favorable temperature was maintained for a long period of time while the crystals were dissolved little by little as about 8 hours, and 14 hours in total till the temperature reached 25 °C and 28 °C, respectively.

[0051] The sample was left in a room at 10 °C again, and observed for the state. As the result, the crystals were fine and the refrigerant was in the state of slurry. The sample was left as it is for one week, but the state hardly changed, and no conglomeration was observed.

[0052] As the result of further observation, crystals with a particle diameter of 3 to 6 mm were found in some parts only after 7 days.

EXAMPLE 3

[0053] A sample of a cooling pillow was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 200 g, as anhydride, of disodium hydrogenphosphate, 36 g, as anhydride, of sodium ammonium hydrogenphosphate, and 35 g, as anhydride, of diammonium hydrogenphosphate to make a mixture of 1300 g in total.

[0054] As the result of carrying out a test on said sample under the same conditions as in Example 1, favorable temperature was maintained for a long period of time while the crystals were dissolved little by little as about 8 hours, and 14 hours in total till the temperature reached 25 °C and 28 °C, respectively.

[0055] The sample was left in a room at 10 °C again, and observed for the state. As the result, the crystals were fine and the cooling agent was in the state of slurry. The sample was left as it is for one week, but the state hardly changed, and no conglomeration was observed.

[0056] As the result of further observation, crystals with a particle diameter of 4 to 8 mm were found in some parts only after 5 days.

EXAMPLE 4

[0057] A sample of a cooling pillow was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 240 g, as anhydride, of disodium hydrogenphosphate, 78 g, as anhydride, of diammonium hydrogenphosphate, and, in addition, 1 g of strontium hydroxide as nucleating agent to make a mixture of 1300 g in total.

[0058] As the result of carrying out a test on said sample under the same conditions as in Example 1, favorable temperature was maintained for a long period of time while the crystals were dissolved little by little as about 8 hours, and 14 hours in total till the temperature reached 25 °C and 28 °C, respectively.

[0059] The sample was left in a room at 10 °C again, and observed for the state. As the result, fine needle-like crystals were precipitated out, and the cooling agent was in the state of slurry. The sample was left as it is for one week, but the state hardly changed. Also after 3 months, the state hardly changed too, and no conglomeration was observed.

[0060] As the result of further observation, crystals with a particle diameter of 4 to 8 mm were found in some parts only after 15 days.

EXAMPLE 5

[0061] A sample of a cooling pillow was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 240 g, as anhydride, of disodium hydrogenphosphate, 78 g, as anhydride, of diammonium hydrogenphosphate, and, in addition, 2 g of lithium hydroxide as the nucleating agent to make a mixture of 1300 g in total.

[0062] As the result of carrying out a test on said sample under the same conditions as in Example 1, favorable temperature was maintained for a long period of time while the crystals were dissolved little by little as about 8 hours, and 14 hours in total till the temperature reached 25 °C and 28 °C, respectively.

[0063] The sample was left in a room at 10 °C again, and observed for the precipitating state of crystal. As the result, fine crystals were precipitated, and the cooling agent as the whole came to be in the state of slurry. The sample was left as it is for one week, but the state hardly changed. Also after three months, it hardly changed, and no conglomeration was observed.

[0064] As the result of further observation, crystals with a particle diameter of 3 to 6 mm were found in some parts only after one month.

EXAMPLE 6

[0065] A sample was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 240 g, as anhydride, of disodium hydrogenphosphate, 78 g, as anhydride, of diammonium hydrogenphosphate, and in addition, 2 g of dihydrate of calcium hydrogenphosphate as the nucleating agent to make a mixture of 1300 g in total.

[0066] As the result of carrying out a test under the same conditions as in Example 1, favorable temperature was maintained for a long period of time while the crystals were dissolved little by little as about 8 hours, and 14 hours in total till the temperature reached 25 °C and 28 °C, respectively.

[0067] The sample was left in a room at 10 °C again, and observed for the precipitating state of crystals. As the result, numerous fine crystals were precipitated, and the cooling agent as the whole became slurry. The sample was left as it is for one week, but the state hardly changed. Also after 3 months, the state hardly changed, and no conglomeration was observed.

[0068] As the result of further observation, crystals with a particle diameter of 3 to 6 mm were found in some parts only after 1 month.

EXAMPLE 7

[0069] A sample was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 240 g, as anhydride, of disodium hydrogenphosphate, 78 g, as anhydride, of diammonium hydrogenphosphate, and in addition 2 g of dihydrate of calcium hydrogenphosphate as the nucleating agent , and 9 g of SANWET IM-500D (produced by SANYO CHEMICAL INDUSTRIES, LTD.) as the highly water absorbent polymer to make a mixture of 1300 g in total.

[0070] As the result of carrying out a test on said sample under the same conditions as in Example 1, favorable temperature was maintained for a long period of time while the crystals were dissolved little by little as about 8 hours, and 14 hours in total till the temperature reached 25 °C and 28 °C, respectively.

[0071] The sample was left in a room at 10 °C again, and observed for the precipitating state of crystals. As the result, numerous fine crystals were precipitated, and the cooling agent as the whole became somewhat viscous slurry, and the sample had a soft touch. The sample was left as it is for one week, but the state hardly changed. As the result of similar observations after 3 months and 6 months, the state hardly changed, and no conglomeration was observed.

[0072] After further observation, crystals with a particle diameter of 3 to 6 mm were found in some parts only after 1 month.

EXAMPLE 8

[0073] A sample was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 120 g, as anhydride, of sodium phosphate, 120 g, as anhydride, of ammonium dihydrogenphosphate, and in addition 2 g of dihydrate of calcium hydrogenphosphate as the nucleating agent, and 6 g of SANFRESH^R ST-500MPS (fine powder-type, produced by SANYO CHEMICAL INDUSTRIES, LTD.) as the highly water absorbent polymer to make a mixture of 1300 g in total.

[0074] As the result of carrying out a test on said sample under the same conditions as in Example 1, favorable temperature was maintained for a long period of time while the crystals were dissolved little by little as about 9 hours, and 16 hours in total till the temperature reached 25 °C and 30 °C, respectively.

[0075] The sample was left in a room at 10 °C again, and observed for the precipitating state of crystals. As the result, numerous fine crystals were precipitated, and the cooling agent as the whole became somewhat viscous slurry, and the sample had a soft touch. The sample was left as it is for one week, but the state hardly changed. As the result of similar observations after 3 months, and 9 months, the state hardly changed, and no conglomeration was observed.

[0076] After further observation, crystals with a particle diameter of 4 to 8 mm were found in some parts only after 1 month.

EXAMPLE 9

[0077] A sample was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 240 g, as anhydride, of disodium hydrogenphosphate, 78 g, as anhydride, of diammonium hydrogenphosphate, and in addition 2 g of dihydrate of calcium hydrogenphosphate as the nucleating agent, and 9 g of SANFRESH^R ST-500MPS (produced by SANYO CHEMICAL INDUSTRIES, LTD.) as the highly water absorbent polymer to make a mixture of 1300 g in total.

[0078] As the result of carrying out a test on said sample under the same conditions as in Example 1; favorable temperature was maintained for a long period of time while the crystals were dissolved little by little as about 9 hours, and 16 hours in total till the temperature reached 25 °C and 30 °C, respectively.

[0079] The sample was left in a room at 10°C again, and observed for the precipitating state of crystals. As the result, numerous fine crystals were precipitated, and the cooling agent as the whole became somewhat viscous slurry, and the sample had a soft touch. The sample was left as it is for one week, but the state hardly changed. As the result of similar observations after 3 months, 6 months and 9 months, the state hardly changed, and no conglomeration was observed.

EXAMPLE 10

[0080] A sample of cooling pillow was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 194 g, as anhydride, of sodium dihydrogenphosphate, 65 g of sodium hydroxide, 78g, as anhydride, of diammonium hydrogenphosphate, and in addition 1 g of strontium hydroxide as the nucleating agent to make a mixture of 1300 g in total.

[0081] As the result of carrying out a test on said sample under the same conditions as in Example 1, favorable temperature was maintained for a long period of time while the crystals were dissolved little by little as about 8 hours, and 15 hours in total till the temperature reached 25 °C and 30 °C, respectively.

[0082] The sample was left in a room at 10 °C again, and observed for the precipitating state of crystals. As the result, fine needlelike crystals were precipitated, and the cooling agent as the whole became slurry. The sample was left as it is for one week, but the state hardly changed, and no conglomeration was observed.

[0083] As the result of similar observations after 3 months, the state hardly changed. Fifteen days after that, crystals with particle diameter of 4 to 8 mm were first observed in some parts.

EXAMPLE 11

[0084] A sample of cooling pillow was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 185 g, as anhydride, of trisodium phosphate, 55 g of phosphoric acid, 78 g, as anhydride, of diammonium hydrogenphosphate, and in addition 2 g of calcium hydroxide as the nucleating agent to make a mixture of 1300 g in total.

[0085] As the result of carrying out a test on said sample under the same conditions as in Example 1, favorable temperature was maintained for a long period of time while the crystals were dissolved little by little as about 8.5 hours, and 15.5 hours in total till the temperature reached 25 °C and 30 °C, respectively.

[0086] The sample was left in a room at 10 °C again, and observed for the precipitating state of crystals. As the result, fine crystals were precipitated, and the cooling agent as the whole became slurry. The sample was left as it is for one week, but the state hardly changed, and no conglomeration and the like was observed.

[0087] As the result of similar observations after 3 months, the state hardly changed, and no conglomeration was observed. One month after that, crystals with particle diameter of 4 to 8 mm were first observed in some parts.

COMPARATIVE EXAMPLE 1

[0088] A sample was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 324 g, as anhydride, of disodium hydrogenphosphate to make a mixture of 1300 g in total.

[0089] As the result of carrying out a test on said sample under the same conditions as in Example 1, the temperature of the sample reached 25 °C after about 4 hours, and 28 °C after 10 hours.

[0090] After the observation of the state of the recrystallization in the same manner as in Examples, a large number of comparatively large crystals with particle diameter of 6 to 12 mm were produced. The sample was left as it is for one week, and then the crystals had grown to form conglomerations, which could not be broken by simple pressing with fingers.

COMPARATIVE EXAMPLE 2

[0091] A sample was made in the same manner as in Example 1 except for using a cooling agent prepared by adding ion-exchanged water to 380 g, as anhydride, of sodium sulfate to make a mixture of 1300 g in total.

[0092] As the result of carrying out a test on said sample under the same conditions as in Example 1, the temperature of the sample reached 25 °C after about 2 hours, and 28 °C after 6 hours.

[0093] After the observation of the state of the recrystallization in the same manner as in Examples, a great number of conglomerations of crystals still larger than those of Comparative Example 1 had grown up. These could not be broken by a striking with hands, and a stronger strike broke the bag to let the solution leak out.

Claims

1. Use of a mixture of (i) at least one sodium phosphate salt selected from disodium hydrogenphosphate, sodium dihydrogenphosphate, and trisodium phosphate and hydrates thereof, (ii) at least one sodium ammonium phosphate salt or one ammonium phosphate salt selected from sodium ammonium hydrogenphosphate, diammonium hydrogenphosphate, ammonium dihydrogenphosphate, ammonium phosphate and hydrates thereof, and (iii) water in a cooling agent composition containing 5 to 60% by weight of the phosphate salts in the anhydride form.

2. Use of a mixture as defined in Claim 1 wherein the proportion of Na to NH₄ group (Na/NH₄) contained in the cooling agent is 1 : 5 to 5 : 1 in molar ratio, and the total molar ratio of Na group and NH₄ group to 1 mol of PO₄ group [(Na+NH₄)/PO₄] is 1 : 1.5 to 1 : 2.5.

3. Use of a mixture as defined in Claim 1 wherein the sodium phosphate salt is disodium hydrogenphosphate or the hydrate thereof, and the sodium ammonium phosphate salt or ammonium phosphate salt is sodium ammonium hydrogenphosphate or diammonium hydrogenphosphate or the hydrates thereof.

4. Use of a mixture as defined in Claim 1 which is obtainable by adding 0.01 to 5% by weight, in respect of the whole cooling agent, of at least one nucleating agent selected from the group consisting of each phosphate or hydroxide of lithium and alkaline earth metals and the hydrates thereof.

5. Use of a mixture as defined in Claim 4 wherein the nucleating agent is calcium phosphate salt, strontium phosphate salt, calcium hydroxide, strontium hydroxide, or hydrate thereof.

6. Use of a mixture as defined in Claim 1 which is obtainable by adding one substance selected from the group consisting of a highly water absorbent polymer, a thickener, and a polymeric flocculant in a proportion of 0.01 to 3% by weight in respect of the whole cooling agent.

7. A cooling pillow which comprises the mixture defined in any of Claims 1 to 6 sealed in a synthetic resin bag.

Ansprüche

1. Verwendung einer Mischung aus (i) mindestens einem Natriumphosphatsalz, gewählt aus Dinatriumhydrogenphosphat, Natriumdihydrogenphosphat und Trinatriumphosphat und Hydraten davon, (ii) mindestens einem Natriumammoniumphosphatsalz oder einem Ammoniumphosphatsalz, gewählt aus Natriumammoniumhydrogenphosphat, Diammoniumhydrogenphosphat, Ammoniumdihydrogenphosphat, Ammoniumphosphat und Hydraten davon, und (iii) Wasser in einer Kühlmittelzusammensetzung, die 5 bis 60 Gew.-% der Phosphatsalze in Anhydridform enthält.

2. Verwendung einer Mischung gemäß Anspruch 1, wobei das Verhältnis von Na zur NH₄-Gruppe (Na/NH₄), enthalten in dem Kühlmittel, 1 : 5 bis 5 : 1 als molares Verhältnis beträgt und das molare Gesamtverhältnis der Na-Gruppe und der NH₄-Gmppe zu 1 Mol der PO₄-Gruppe [(Na + NH₄) /PO₄] 1 : 1,5 bis 1 : 2,5 beträgt.

3. Verwendung einer Mischung gemäß Anspruch 1, worin das Natriumphosphatsalz Dinatriumhydrogenphosphat oder das Hydrat davon und das Natriumammoniumphosphatsalz oder Ammoniumphosphatsalz Natriumammoniumhydrogenphosphat oder Diammonhmhydrogenphosphat oder die Hydrate davon sind.

4. Verwendung einer Mischung gemäß Anspruch 1, welche erhältlich ist durch Hinzusetzen von 0,01 bis 5 Gew.-%, bezogen auf das gesamte Kühlmittel, mindestens eines Nukleierungsmittels, gewählt aus der jedes Phosphat oder Hydroxid von Lithium und Erdalkalimetallen und deren Hydrate umfassenden Gruppe.

5. Verwendung einer Mischung gemäß Anspruch 4, wobei das Nukleierungsmittel Calciumphosphatsalz, Strontiumphosphatsalz, Calciumhydroxid, Strontiumhydroxid oder (ein) Hydrat davon ist.

6. Verwendung einer Mischung gemäß Anspruch 1, welche erhältlich ist durch Hinzusetzen eines Substanz, gewählt aus der ein stark wasserabsorbierendes Polymer, ein Verdickungsmittel und ein polymeres Flockungsmittel umfassenden Gruppe, in einem Anteil von 0,01 bis 3 Gew.-%, bezogen auf das gesamte Kühlmittel.

7. Kühlkissen, welches die Mischung gemäß einem der Ansprüche 1 bis 6 in einem Beutel aus synthetischem Harz verschlossen umfaßt.

Revendications

1. Utilisation d'un mélange (i) d'au moins un sel de type phosphate de sodium choisi parmi l'hydrogénophosphate disodique, le dihydrogénophosphate de sodium et le phosphate trisodique et leurs hydrates, (ii) d'au moins un sel de type phosphate de sodium et d'ammonium ou un sel de type phosphate d'ammonium choisi parmi l'hydrogénophosphate de sodium et d'ammonium, l'hydrogénophosphate de diammonium, le dihydrogénophosphate d'ammonium, le phosphate d'ammonium et leurs hydrates, et (iii) d'eau, dans une composition d'agent de refroidissement contenant 5 à 60 % en poids des sels de type phosphate sous la forme d'anhydride.

2. Utilisation d'un mélange tel que défini dans la revendication 1, dans lequel la proportion de groupes Na à NH₄ (Na/NH₄) contenus dans l'agent de refroidissement est de 1:5 à 5:1 en un rapport molaire, et le rapport molaire total du groupe Na et du groupe NH₄ à 1 mole de groupe PO₄ [(Na+NH₄)/PO₄] est de 1:1,5 à 1:2,5.

3. Utilisation d'un mélange tel que défini dans la revendication 1, dans lequel le sel de type phosphate de sodium est l'hydrogénophosphate disodique ou son hydrate, et le sel de type phosphate de sodium et d'ammonium ou le sel de type phosphate d'ammonium est l'hydrogénophosphate de sodium et d'ammonium ou l'hydrogénophosphate de diammonium ou leurs hydrates.

4. Utilisation d'un mélange tel que défini dans la revendication 1, que l'on obtient en ajoutant 0,01 à 5 % en poids, par rapport à l'ensemble de l'agent de refroidissement, d'au moins un agent de nucléation choisi dans le groupe comprenant chacun des phosphates ou hydroxydes de lithium et des métaux alcalino-terreux et leurs hydrates.

5. Utilisation d'un mélange tel que défini dans la revendication 4, dans lequel l'agent de nucléation est un sel de phosphate de calcium, un sel de phosphate de strontium, l'hydroxyde de calcium, l'hydroxyde de strontium ou leurs hydrates.

6. Utilisation d'un mélange tel que défini dans la revendication 1, que l'on obtient en ajoutant une substance choisie dans le groupe comprenant un polymère à haute absorption d'eau, un agent épaississant et un floculant polymère, dans une proportion de 0,01 à 3 % en poids par rapport à l'ensemble de l'agent de refroidissement.

7. Coussin de refroidissement qui comprend le mélange tel que défini dans l'une quelconque des revendications 1 à 6, hermétiquement fermé dans un sac en résine synthétique.